Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP307983.RAFaA7VHhTvguXTWxiGqnMj_EGlSLfP9V1s-MIRAVztgs130_assertion> ?p ?o ?g. }
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- NP307983.RAFaA7VHhTvguXTWxiGqnMj_EGlSLfP9V1s-MIRAVztgs130_assertion type Assertion NP307983.RAFaA7VHhTvguXTWxiGqnMj_EGlSLfP9V1s-MIRAVztgs130_head.
- NP307983.RAFaA7VHhTvguXTWxiGqnMj_EGlSLfP9V1s-MIRAVztgs130_assertion description "[Inactivating mutations of CDKN1B, encoding the p27 cyclin-dependent kinase inhibitor, were reported to cause hyperparathyroidism in a multiple endocrine neoplasia type 1-like syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP307983.RAFaA7VHhTvguXTWxiGqnMj_EGlSLfP9V1s-MIRAVztgs130_provenance.
- NP307983.RAFaA7VHhTvguXTWxiGqnMj_EGlSLfP9V1s-MIRAVztgs130_assertion evidence source_evidence_literature NP307983.RAFaA7VHhTvguXTWxiGqnMj_EGlSLfP9V1s-MIRAVztgs130_provenance.
- NP307983.RAFaA7VHhTvguXTWxiGqnMj_EGlSLfP9V1s-MIRAVztgs130_assertion SIO_000772 18288099 NP307983.RAFaA7VHhTvguXTWxiGqnMj_EGlSLfP9V1s-MIRAVztgs130_provenance.
- NP307983.RAFaA7VHhTvguXTWxiGqnMj_EGlSLfP9V1s-MIRAVztgs130_assertion wasDerivedFrom befree-20150227 NP307983.RAFaA7VHhTvguXTWxiGqnMj_EGlSLfP9V1s-MIRAVztgs130_provenance.
- NP307983.RAFaA7VHhTvguXTWxiGqnMj_EGlSLfP9V1s-MIRAVztgs130_assertion wasGeneratedBy ECO_0000203 NP307983.RAFaA7VHhTvguXTWxiGqnMj_EGlSLfP9V1s-MIRAVztgs130_provenance.